# FDA Inspection 674222 - MEDLINE RENEWAL - August 03, 2010

Source: https://www.keypedia.com/records/fda_inspections/medline-renewal/9d26adcf-85f1-4945-9448-6db6d40d911e
Source feed: FDA_Inspections

> FDA Inspection 674222 for MEDLINE RENEWAL on August 03, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 674222
- Company Name: MEDLINE RENEWAL
- Inspection Date: 2010-08-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 674222 - 2010-08-03](https://www.keypedia.com/records/fda_inspections/medline-renewal/8d61ad82-6e12-4f44-8fba-646ec855689c)
- [FDA Inspection 590921 - 2009-06-02](https://www.keypedia.com/records/fda_inspections/medline-renewal/82af096e-f856-41b2-8b79-1b46c2ef1b41)

Company: https://www.keypedia.com/companies/medline-renewal/808c5e60-c028-4a73-8e58-fbbe7ec1c5fa

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7